合成高硫胺糖醇缩醛(II),[3-(4'-氨基-2'-甲基-嘧啶基-(5')-甲基)-4-甲基-5-(β,γ-二氧丙基)-噻唑氯-盐酸盐],二(3-)(4'-氨基-2'-甲基-嘧啶基-(5')-甲基)-4-甲基-5-烯丙基-噻唑氯盐酸盐(VIII)。Erthate Verbindung ist(nach WH Schopfer)与抗微生物剂Thiamins的组合。
合成高硫胺糖醇缩醛(II),[3-(4'-氨基-2'-甲基-嘧啶基-(5')-甲基)-4-甲基-5-(β,γ-二氧丙基)-噻唑氯-盐酸盐],二(3-)(4'-氨基-2'-甲基-嘧啶基-(5')-甲基)-4-甲基-5-烯丙基-噻唑氯盐酸盐(VIII)。Erthate Verbindung ist(nach WH Schopfer)与抗微生物剂Thiamins的组合。
Certain imidazo[1,2-a]pyridines useful in the treatment of ulcers
申请人:Fujisawa Pharmaceutical Co., Ltd.
公开号:US04725601A1
公开(公告)日:1988-02-16
Certain imidazo[1,2-a]heterocyclic compounds useful in the treatment of ulcers are provided.
提供了一些在溃疡治疗中有用的咪唑并[1,2-a]杂环化合物。
MACROCYCLIC INHIBITORS OF FLAVIVIRIDAE VIRUSES
申请人:Gilead Sciences, Inc.
公开号:US20150274774A1
公开(公告)日:2015-10-01
Provided are compounds of Formula I:
and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of virus infections, particularly hepatitis C infections.